-- 

*Dear Associates !*

I am *Ahmed from Sage Group Consulting, Inc*, Please find the job
descriptions below and if you are interested and available for this
position please *send me your updated resume* along with contact number.

*Please send me resume to z <[email protected]>[email protected]
<[email protected]>*



*SAS PROGRAMMER *

*Woodcliff, NJ*

*12 months +*

*Phone & In-person*

*$55-60/hr*



*Responsibilities*

   - Responsible for SDTM data creation and delivery for oncology studies.
   - Prepare SDTM Mapping specification following company standards.
   - Create or participate in SDTM annotation for CRFs/eCRFs for oncology
   trials.
   - Develop programs to create SDTM datasets and Define.xml for
   statistical analysis, tables & listings, and regulatory submissions.
   - Perform Open CDISC validation, coordinate to resolve issues, prepare
   associated documentation.
   - Design and develop SAS macros, applications, and other utilities to
   expedite SAS programming activities and usage by the Oncology Data
   Management and other areas of Clinical for data review.
   - Ensure all programming activities and processes performed are
   conducted according to standard operating procedures, good programming
   practices, and GCP guidelines.

*Qualifications*


   - BS or MS in Computer Science or related field.
   - Five to Seven years of strong experience in programming with clinical
   trial data and developing programs, testing, and documentation
   - Strong SAS programming skills required in Windows and UNIX
   environment, with proficiency in SAS/Base, SAS Macros, SAS/Graph, SQL.
   - Extensive experience of handling SDTM mapping, related data
   structures, and programming to create SDTM data sets.
   - Extensive experience in SDTM validation using OpenCDisc.
   - Good knowledge in developing Define.xml and validation.
   - Extensive experience of handling external data, e.g., laboratory data,
   PK, ECG, Biomarker, Imaging, etc.
   - Good understanding of standards specific to clinical trials, such as
   CDISC, SDTM, MedDRA, WHO DRUG.
   - Good understanding of relational databases, e.g., ORACLE; Knowledge of
   the EDC System, InForm and underlying data structure is a plus.
   - Knowledge of using JReview/IReview is a plus.
   - Strong problem-solving skills.
   - Able to work independently and as a team player; Good organizational,
   time management, and project management skills.
   - Capable of communicating technical concepts.
   - Good understanding of system development life cycles, GCP, and related
   Regulatory guidelines.
   - Should be able to manage the assigned projects independently with
   minimum supervision.


*Thanks and Regards*



*Zulfiqar Ahmed*

*Sage Group Consulting, Inc*

W:+ 732 767 0010 X 704 | Direct: 732 851 1637 |Email: [email protected]

YM: ahmed_maccadin | Gtalk: ahmed.maccadin

LinkedIn: in.linkedin.com/pub/ahmed-zulfiqar/21/950/44b/

Website: www.sageci.com

-- 
You received this message because you are subscribed to the Google Groups 
"Oracle-Projects" group.
To unsubscribe from this group and stop receiving emails from it, send an email 
to [email protected].
To post to this group, send email to [email protected].
Visit this group at http://groups.google.com/group/oracle-projects.
For more options, visit https://groups.google.com/d/optout.

Reply via email to